A study testing whether a GLP-1 medicine from Lilly, orforglipron, can help with weight.
- Who can join
- Children and teens 12 to 17, have obesity.
- What you take
- orforglipron, given as part of the study at no cost to you. Some participants may receive a placebo (an inactive version) instead, decided at random.
- How long it lasts
- The full study runs about 6.2 years; your own time in it is usually shorter.
- What you get
- The study medication and study-related care at no cost. Compensation varies by study site; many cover travel and provide the study medication at no cost. The trial coordinator will explain what that site offers before you join.
What this study is for
Full study title: A Study of Orforglipron (LY3502970) in Adolescent Participants With Obesity, or Overweight With Related Comorbidities.
Primary condition: Obesity. Also studied in: Overweight.
Who can join, in detail
Key inclusion criteria
- Have a history of at least 1 unsuccessful effort to lose sufficient body weight after participation in a structured lifestyle modification program (diet and exercise counseling for at least 3 months) prior to screening.
- Obesity as defined by BMI equal to or above the 95th percentile for age and sex (on age- and gender-specific growth chart [CDC-NCHS, 2022]); OR
- Overweight as defined by BMI equal to or above the 85th percentile but less than the 95th percentile for age and sex, on age- and sex-specific growth chart (CDC-NCHS, 2022), and at least 1 weight-related comorbidity,
- hypertension
- type 2 diabetes (T2D)
Key exclusion criteria
- Prepubertal (Tanner stage 1)
- Have a self-reported, or by parent or legal guardian where applicable, decrease in body weight greater than 5 kilograms (kg) (11 pounds) within 90 days before screening
- Have undergone or plan to undergo weight reduction procedure during the study, such as, but not limited to:
- gastric bypass
- sleeve gastrectomy
Where this study is enrolling
This trial has 14 US sites across 12 states. Contact the site coordinator directly to start the screening process.
California
- Carey Chronis MD Pediatric, Infant and Adolescent MedicineVentura, California805-642-4704
Connecticut
- Stamford Therapeutics ConsortiumStamford, Connecticut727-544-4842
Georgia
- Children's Healthcare of Atlanta - Center for Advanced PediatricsAtlanta, Georgia404-712-4731
Illinois
- Ann & Robert H. Lurie Children's Hospital of ChicagoChicago, Illinois312-503-1499
Louisiana
- Velocity Clinical ResearchLafayette, Louisiana337-519-4742
Mississippi
- MedPharmics, LLCGulfport, Mississippi228-206-1283
Missouri
- Sundance Clinical ResearchSt Louis, Missouri314-567-3377
North Carolina
- Lucas Research, Inc.Morehead City, North Carolina252-222-5700
Pennsylvania
- Childrens Hospital of PittsburghPittsburgh, Pennsylvania412-692-6935
Tennessee
- Vanderbilt Health One Hundred OaksNashville, Tennessee615-322-6000
Texas
- Dynamed Clinical Research, LP d/b/a DM Clinical ResearchHouston, Texas
- La Providence Pediatrics Clinic - Chemidox Clinical TrialsHouston, Texas833-324-3643
- Martin Diagnostic ClinicTomball, Texas
Utah
- Velocity Clinical Research, Salt Lake CitySouth Jordan, Utah
Timeline
Started enrolling: 2024-11-18. Expected completion: 2031-01. Last updated on ClinicalTrials.gov: 2026-05-27.
Official source
We sync this data quarterly from ClinicalTrials.gov, the federal registry for clinical research. Before contacting a site, verify the trial is still recruiting on the official page:
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